Prevalence and associated factors of schistosomiasis among pregnant women in northern Senegal

Background Schistosomiasis remains a public health concern worldwide. It is responsible for more than 240 million cases in 78 countries, 40 million of whom are women of childbearing age. In the Senegal River basin, both Schistosoma haematobium and Schistosoma mansoni are very prevalent in school-age children. However, there is a lack of information on the burden of schistosomiasis in pregnant women, which can cause complications in the pregnancy outcome. This study aimed to determine the prevalence and associated factors of schistosomiasis in pregnant women. Methods We conducted a prospective cross-sectional study of pregnant women attending antenatal clinics at the health center of the Senegalese Sugar Company and at the hospital of Richard Toll between August and December 2021. The urine and stool samples collected were examined using microscopy techniques and quantitative polymerase chain reaction (qPCR) to detect the presence of S. haematobium and S. mansoni. The urines were previously tested using urine reagent strips to detect hematuria and proteinuria. Socio-demographical, clinical, and diagnostically data were recorded by the midwife and the gynaecologist. The data were analyzed using a logistic regression model. Results Among the 298 women examined for the infection by microscopic, 65 (21.81%) were infected with urogenital schistosomiasis, 10 (3.36%) with intestinal schistosomiasis, and 4 (1.34%) were co-infected with both types of schistosomiasis. Out of the 288 samples tested by qPCR, 146 (48.99%) were positive for S. haematobium, 49 (35.51%) for S. mansoni and 22 (15.94%) for both species (co-infection). Pregnant women having microscopic haematuria and proteinuria were significantly more infected (p < 0.05). Conclusion This study has revealed a high prevalence of schistosomiasis in pregnant women in Senegal. The qPCR allowed us to detect more cases compared to the microscopy. There is a need to conduct more studies to understand the real burden of the disease and to set up a surveillance system to prevent pregnancy-related complications.


Background
Schistosomiasis is a group of chronic tropical diseases caused by parasitic worms of the genus Schistosoma [1].Schistosoma haematobium and Schistosoma mansoni causing respectively urogenital and intestinal schistosomiasis, are the most prevalent in sub-Saharan Africa [2].Transmission of schistosomiasis has been reported in 91 countries worldwide [3] and it is the second most endemic parasitic disease in the world after malaria [4].In 2021, schistosomiasis preventive chemotherapy was required in 51 countries, for a total of 251.4 million people including 136 million School age children and 115.4 million adults [3].Mortality due to the disease and the number of persons at risk were respectively estimated at 200,000 and 700 million [5].The school age children are the most affected group due to their frequent contact with the water infested by Schistosoma larvae excreted by snail intermediate hosts belonging to the genus Bulinus and Biomphalaria [6,7].Females, in particular, are more likely to be exposed to the infection because of frequent domestic activities carried out in infested water [8,9] such as washing clothes, fetching water, and bathing in addition to drinking and laundry [9].
It is estimated that over 40 million of women of reproductive age are affected by schistosomiasis worldwide, with approximately 10 million infected per year during pregnancy in Africa [10].These data are mostly based on results of standard microscopy [11][12][13] and few studies used molecular or immunological techniques [14][15][16] to detect Schistosoma infection in urine or stool samples.
Schistosomiasis control targets implemented by national control programs, focus exclusively on preventive chemotherapy on school-aged children using Praziquantel (PZQ), the only anthelmintic available and effective against schistosomiasis [17].Therefore, despite the high burden of schistosomiasis during pregnancy, women of reproductive age are not systematically included in mass treatment campaigns, even though studies have demonstrated the safety of PZQ for pregnant women [18,19] and the recommendation of the World Health Organization (WHO) to include pregnant women in Mass Drug Administration [18].
Studies in other countries have reported significant association of schistosomiasis and adverse pregnancy outcomes parameters (miscarriage, stillbirth, preterm, and small-for-gestational age) and also other clinical parameters (low birth weight delivery, neonatal death, or length for age Z scores) [20,21].
In northern Senegal, particularly in the Senegal River basin, the rapid evolution of the epidemiological system has led to an explosion of schistosomiasis, with S. mansoni and S. haematobium becoming co-endemic [22,23].The presence of irrigation canals, the proximity and regular frequentation of water points are often cited as the main risk factors for school-age children and adults [8].However, few data are available about the factors associated with the contamination of pregnant women in this part of Senegal.Thus, this study assessed the prevalence and intensity of the schistosomiasis infection and the associated factors in pregnant women attending antenatal care in the District of Richard Toll in northern Senegal.

Study area
This study was carried out in two health facilities: a private health center named Senegalese Sugar Company health center (CSS) and a public health center named Secondary Public Health Establishment (EPS) both located in the district of Richard Toll (16°27′44″ North and 15°42′02″ West) at 108 km from the Saint-Louis region in northern Senegal (Fig. 1).Population increased from 48,968 in 2007 to 60,127 in 2014 [24]. .The climate is tropical with a short rainy season and long dry season [25].Average annual precipitations were about 215 mm and temperatures varied between 30 °C and 39 °C [25].
Intestinal and urogenital schistosomiasis were endemic in the district a few years after the construction of the Diama dam in 1986 [24].The area is mainly characterized by the Taouey canal linking the Senegal River to the Lake of Guiers and several secondary irrigation canals for agricultural activities [26].Although many households have access to tap water, most of the activities implicating water are done by the population on the banks of the river, Taouey and secondary canals for domestic and recreational activities [27].

Study design and period
We carried out a prospective cross-sectional study during five months from August 2021 to December 2021 in the CCS and EPS health facilities.The study was done in collaboration with midwife and gynecologist of each facility.All pregnant women who come for the first time at the health facility and those who were in their first, second, and third trimester antenatal care were enrolled based on the consultation register at the two health facilities.

Study population and participant selection
The study population consisted of pregnant women aged between 14 and 43 years attending antenatal care at the CSS and EPS health facilities.Participants were selected based on the daily register of consultation used by the midwife during the four months of study recruitment.After identification based in the name of participant in the register, the study was explained to each woman before asking to sign consent to participate in the study.

Collection of sociodemographic, clinical and paraclinical data
After consent signature, a validated questionnaire designed one android tablet using the Open Data Kit (ODK) platform was administered to each participant.The health worker responsible for the welcoming of patients registered the information on identity and age.The study team collected the other demographic and socio-economic information (locality, marital status, educational level and economical activities), source of water (lake, canal, river, basin water, and backwater) and woman behavior in relation to the water bodies (drinking, laundry, bathing, household water source and other use).The other information related to schistosomiasis infection and treatment history with PZQ, clinical parameters (history of haematuria and schistosomiasis infection, type of treatment or drug administered within the last 6 months), the possession of a health booklet were also collected during sampling.The other clinical data were collected by the gynecologist.Parity and birth weight were recorded in the health booklet and women were telephoned after childbirth to obtain pregnancy outcome and birth weight.

Sample collection
Each participant interviewed received two pre-labeled sterile containers of 60 ml for urine, stool with the identification number, and asked to give urine and stool samples as soon as possible between 10:00 am and 2:00 pm corresponding to the health facilities consultation time.Before giving the container, each participant was briefed on the importance of sample collection at this time and then asked when possible, to give the totality of urine.

Macroscopic and microscopic examination of urine and stool samples Urine examination
The first step was the macroscopic observation followed by the screening of the haematuria, proteinuria, presence of nitrites and leucocytes in urine sample using reagent strips for urinalysis (Siemens Healthcare Diagnostics Inc. Tarrytown, NY 10,591 − 5097 USA).In a second step, S. haematobium eggs were searched in urine using the filtration method described by Plouvier et al. [28].Briefly, each urine sample was gently shaken to ensure homogenization of the eggs before filtering 10 ml of the liquid through a Swinnex® filter.Filters were observed under a microscope after deposited a drop of lugol's iodine in order to visualize the eggs.The number of S. haematobium eggs per 10 ml of urine (infection intensity) was recorded.The infection intensity after microscopic examination for S. haematobium was classified as light (1-49 eggs/10 ml of urine) or heavy (≥ 50 eggs/10 ml of urine) [29].

Stool examination
S. mansoni eggs were screened in stool samples using the Kato-Katz technique as described in the WHO guideline Fig. 1 Location of the study sites and the two health facilities [30].Two Kato-Katz thick smears of 41.7 mg of stool were prepared and read 24 h later under a microscope.As it is difficult to shake the stools to homogenize them like the urine sample, we took 41.7 mg in two different corners of the stool to increase the chances of detecting eggs.For S. mansoni, the number of eggs per gram of faeces (epg) was calculated by multiplying the mean egg count of the two slides by 24.The infection intensity was classified as light (1-99 epg), moderate (100-399 epg) and high (≥ 400 epg) [31].For each urine and stool sample, one aliquot was prepared in 1.5 ml Eppendorf tube and conserved at -20 °C in order to confirm the diagnostic by molecular biology.

Molecular diagnostic DNA extraction in urine and stool
For both urine and stool, the DNA extraction was done by the same extraction kit.A 200 µl volume of urine and a mince up to 30 mg of stool were centrifuged separately in a 1.5 ml Eppendorf tube.DNA was extracted from the pellet using the EZNA® Tissue DNA Kit (Omega Bio-tek, USA) following the manufacture recommendations.The extracts DNA were stored at -20 °C until use.

DNA detection and quantification by polymerase chain reaction (qPCR)
The S. haematobium Dra1 gene previously described by Hamburger et al. [32] was targeted by qPCR technique.Primers and probes sequences used were Sh-RV: 5′-TCA-CAA-CGA-TAC-GAC-CAA-C-3′; Sh-FW: 5′-GAT-CTC-ACC-TAT-CAG-ACG-AAA-C-3′; Shprobe: 5'-FAM-TGT-TGG-TGG-AAG-TGC-CTG-TTT-CGC-AA-TAMRA-3' .Dra1 qPCR was performed with a 20 µl reaction mix containing 5 µl of DNA, 3.5 µl of sterile ultrapure water, 0.5 µl of each primer, 0.5 µl of Taq-ManTM probe (Applied Bio-systems, Foster City, CA, USA), and 10 µl of the ROCHE® Master mix Master Mix.The DNA amplification was performed on a CFX96 thermal cycler (Bio-Rad).The thermocycler program consisted by an initial denaturation and purification step of 5 min at 95 °C followed by denaturation step of 39 cycles of 30 s at 95 °C, and a hybridization step of 60 s at 60 °C.DNA quantification was expressed on the basis of cycle threshold (Ct) value.At each assay, a negative control and a positive S. haematobium group control between 18 and 23 Ct value were used.Any sample with a Ct < 35 was considered as positive.DNA from S. haematobium adult worm of the VITROME lab of Dakar was used as positive control for S. haematobium.S. mansoni DNA was detected by qPCR, targeting a highly repeated 121-bp sequence of S. mansoni (Sm1-7) described by Wichmann et al. [33].Primers sequences used were: SRA1: 5

'-C C A C G C T C T C G C A A A T A A T C T-3' and SRS2: 5'-C A A C C G T T C T A T G A A A A T C G T T
G T-3.The probes sequences were SRP: 5'-FAMTCC-GAAACCACTGGACGGATTTTTATGAT-TAMRA-3' [34].The qPCR was performed with a 20 µl reaction mixture containing 5 µl of DNA, 3.5 µl of sterile ultrapure water, 0.5 µl of each primer, 0.5 µl of TaqManTM probe and 10 µl of Master Mix.Positive control for S. mansoni was obtained from the VITROME lab at the Aix-Marseille University.The reaction was performed on a CFX96 thermal cycler (BIO-RAD), with the program consisting of an initial purification step of 2 min at 50 °C followed by denaturation for 10 min at 95 °C, hybridization for 40 cycles at 95 °C for 15 s, and 60 °C for 1 mn sampling maintained at 4˚C.DNA detection was expressed as the cycle threshold (Ct) value.At each assay, a negative and a positive S. mansoni control (18 < Ct < 23) were used.Any sample with a Ct < 35 was considered positive.

Statistical analysis
For both urine and stool examination, a participant was considered as positive if she had microscopic and/or qPCR positive.Statistical analysis was done using Stata software version 14.0 (College Station, Texas, USA).The comparison of the sensitivity and specificity of the techniques was calculated considering PCR as reference method.The sensitivity was calculated as the positive samples from microscopy divided by the total positive samples from PCR and the specificity as the negative samples issued from microscopy divided by the total negative obtained from the PCR method.In order to search for any statistically significant association between schistosomiasis and the parameters studied, we carried out "logistic regression bivariate analyses".Variables with a p-value < 0.2 in bivariate analyses were integrated in multivariate analyses.Multivariate analyses were performed using a logistic regression model.Step-wise elimination of variables was performed based on the variables with high p-value and AIC (Akaike information criterion) in the final model.The significance level was fixed at p-value = 0.05 in the final model.

Characteristics of the study population
A total of 298 pregnant women living in Richard Toll and surrounding villages took part in the study.The total number of pregnant women who attended the antenatal clinic at the EPS was 232 (77.85%) and 66 (22.15%) at the CSS.Majority of the participants were married 286 (95.97%) and were aged from 20 to 35 years 213 (71.48%).They were divided into three age groups: 14 to 19 years 55 (18.46%), between 20 and 35 years 213 (71.48%) and > 35 years 30 (10.07%).The majority of women were illiterate 159 (53.36%).The frequencies of education levels were primary school 53 (17.79%), secondary school 59 (19.80%) and high school, 27 (9.06%).Most of the women had no income-generating activity (79.19%).The other characteristics of this study, i.e. women's attitudes to water and clinical and diagnostical parameters, are detailed in Table 1.

Prevalence and intensity of schistosoma infection according to the different techniques
Urine filtration technique Out of the 298 urine samples from pregnant women analyzed by urine filtration method, a total of 65 (21.81%) were positive to urogenital schistosomiasis.The intensity of infection was low with 87.7% excreting less than 49 eggs/10 ml of urine.The maximum egg load was 200 eggs/10 ml of urine.
Kato Katz technique A total of 142 stool samples were recorded among the 298 participants.Among them, 10 (7.04%) were positive for S. mansoni by the Kato-Katz technique with low intensity of infection as all women excreting less than 8 eggs/gram.Only 4 (2.82%) pregnant women were co-infected with S. haematobium and S. mansoni (Table 2).

QPCR technique
The qPCR detected 81 and 38 cases missed respectively by the urine filtration (UF) and Kato-Katz (KK) techniques.Molecular prevalence was high for S. haematobium (n = 146; 48.99%) and S. mansoni (n = 49; 35.51%), as well as for co-infection (n = 22; 15.94%) (Table 2).The results on sensitivity and specificity of each technique in the detection of S. haematobium and S. mansoni in pregnant women are summarized (Table 3).

Bivariate analysis Socio-demographic factors associated with schistosomiasis
Table 4 shows the bivariate analysis between Schistosoma infection detected by microscopic and molecular methods, and socio-demographic factors and history of infection.The results revealed a significant association of S. haematobium infection with the age group of pregnant women.Women aged between 20 and 35 years and those aged over 35 years were significantly protected against S. haematobium infection compared to those aged 14 to 19 years (odds ratio [OR] 0.47; 95% confidence interval (95%CI) 0.25-0.88;p = 0.019 and OR 0.32; 95%CI 0.15-0.93;p = 0.034 for 20-35 and over 35 years old, respectively).

Clinical and diagnostical factors associated with schistosomiasis
Bivariate analysis showed that medium (OR 5.41; 95%CI The women declaring an Intermittent Preventive Treatment with sulfadoxine-pyrimetamine (IPT) within the last 6 months and those with anemia were protected against intestinal schistosomiasis infection (OR 0.46; 95%CI 0.22-0.99;p = 0.048; OR 0.38; 95%CI 0.15-0.99;p = 0.047 respectively), while those with very intense blood in urine had a significant risk of having the intestinal infection (OR 5.15; 95%CI 1.23-21.66;p = 0.049) (Table 4).When considering all cases of schistosomiasis, only medium, intense, and very intense blood in urine and low, medium, and intense proteinuria were significantly associated with having schistosomiasis infection (p < 0.05) (Table 4).

Discussion
This is the first study examining the prevalence of schistosomiasis in pregnant women in Senegal.Using microscopic examination, we identified a high prevalence of S. haematobium 65 (21.81%) and a low prevalence of S. mansoni 10 (7%) in the endemic district of Richard Toll.These differences in prevalence between the two schistosomiasis infections reflect the actual local epidemiological situation in the Senegal River area with S. haematobium becoming more prevalent than S. mansoni in school children [35,36].The opposite of what happened 15 years later after the construction of the Diama dam where S. mansoni was the most prevalent [37][38][39].To our knowledge, the national mean prevalence of S. haematobium and S. mansoni are unclear.However, a study conducted throughout the country showed that the prevalence of S. haematobium ranges from 10% after several PZQ treatments in seasonal transmission focus in central Senegal [40], to more than 90% in the Senegal River basin and the Lake de Guiers [35].However, when considering the district level of Richard Toll, our prevalence of urogenital schistosomiasis is lower than the recent prevalence of 30% and 54%, respectively in 2017 and 2018 in volunteer adults [35].When considering S. mansoni, our prevalence was situated in the interval of 2-20% of the prevalence recently reported in Richard Toll [35], and was so far lower than the 79-100% reported by Webster et al. [23], before recurrent mass PZQ administration by the Senegalese health ministry.Pregnant women have long been excluded from schistosomiasis treatment in Senegal, and therefore limited data on prevalence existed before this study.In addition, in neighboring countries such as Guinea, Mauritania, and Gambia, no studies were available on the prevalence of urogenital schistosomiasis in pregnant women to our knowledge.Only one study was conducted in the neighboring country of Mali with a prevalence of 11% of S. haematobium [41], lower than that reported in the present study.When considering other countries, our prevalence was similar to that reported among Nigerian pregnant women [42], while it's higher than previous prevalence reported in other countries such as Cameroon and Tanzania where the prevalence was less than 5% [12,43].The prevalence of S. haematobium reported in the present study was higher than the mean global prevalence of 13.44% during pregnancy estimated from various countries worldwide [44].This could be explained by the high endemicity of urogenital schistosomiasis in Richard Toll due to the presence of several water contacts, and high prevalence in children and adults despite Mass drug administration of Praziquantel [35,45] .However, the infection rate of S. mansoni in our study was lower than the global prevalence of 12.18% [44] and confirms the patterns of intestinal decrease in the Senegal river basin which is less and less detected by microscopic examination [35].This was not the case in other countries such as Sudan [46] and Tanzania with the second having the highest prevalence of 63.5% in pregnant women [13] probably due to the difference in the sensitivity of the PCR kit used.For both S. haematobium and S. mansoni, the higher rates of low-intensity of infection are in line with what was often reported in previous studies in pregnant women in several countries [13,21,[46][47][48][49][50].This variation in the prevalence in pregnant women reflects the epidemiological character of schistosomiasis which changes strongly across the countries and even in the same country [51][52][53][54] but will also depend on the diagnostic method used.Today, with the availability of genetic markers, molecular diagnosis is often used to increase the possibility of parasite detection by targeting specific DNA fragments.
The majority of molecular diagnostics of Schistosomiasis in pregnant women was generally Blood-PCR-Based and always showed higher prevalence than microscopic techniques with a rate often more than 40% [15].Our results demonstrated high prevalence by urine and stool based on qPCR for both S. haematobium and S. mansoni, respectively compared to microscopic diagnostics.Compared to microscopy, PCRs significantly increased the sensitivity of diagnosis for the detection of S. haematobium and S. mansoni in pregnant women.This ultrasensitivity of qPCR compared to the standard techniques demonstrates its robustness and its performance in comparison with microscopy for the assessment of schistosomiasis prevalence, especially in the case of low prevalence and light egg load, but, also in the prediction of female genital schistosomiasis [55].Quite large numbers of false negatives at microscopy evaluated by the qPCR were certainly due to errors of the microscopic operator rather than storage conditions as the sample was processed the same day of collection.A double microscopy examination of the negative sample would allow having a higher microscopy and permit these women who were considered negative to benefit from treatment.
Bivariate analysis showed that S. haematobium infection was associated with a younger age group.This can be explained by the fact that most women are young and married and in the area of Richard Toll the young mothers (daughters-in-law) are responsible for household domestic activities such as laundry and dishes, which brings them to more frequently in contact with canal and river water.It's known that the prevalence and intensity of schistosomiasis decreases with increasing age [56].In addition, there is evidence that immunity to S. haematobium infection depends on age and therefore affects the prevalence and quantity of eggs in infected individuals [57,58].Our results are in accordance with the previous study in the Richard toll area which found a higher overall prevalence of 95% in 2018 in the young participants aged 5-17 years compared to adult patients (54%), aged 18-75 years [35].Similar results were also observed in Mali, where 11% of pregnant women infected with S. haematobium were aged between 20 and 29 [41], and  also in Nigeria where a higher prevalence of 31.5% % was reported in pregnant women aged 20-24 years [42].
When considering demographic variables, our results show that women attending in the EPS of Richard Toll were significantly more infected than those attending antenatal at the CSS health center.The two structures are located on either side of the Taouey Canal, where women carry out their domestic activities.Although the EPS is closer to the Senegal River, we did not find any significant difference between the women consulting in the two health facilities with respect to the use of water sources.The difference can be attributed to the fact that the EPS is a public establishment that serves pregnant women from various localities in Richard Toll who may not have health insurance.Therefore, they may not receive systematic treatment for schistosomiasis.However, the CSS health center is a private structure that was built by the company for their employees.CSS workers and their families receive systematic treatment for schistosomiasis before and after each agricultural season by the company.Thus, these women were more likely to have a history of treatment of schistosomiasis by PZQ, resulting in a difference in prevalence between the two health facilities.However, more information on the origin of women, the level of access to safe water, and also the length of time in the area, would have allowed a better comprehension of the differences in the prevalence between the two health facilities.
There is no significant difference in the prevalence of schistosomiasis in this study between the levels of education.These results are not in line with the study by Tonga et al. [10] who report that women with higher education levels have more knowledge about the risks of the disease and therefore reduce their contact with infested water making them less infected than the other categories.
The present study showed a significant association between schistosomiasis and income-generating activity.Indeed, unemployed people have more time to do housework than employed people; so, they are for a long time into contact with water and they are more exposed to sources of infection.It was demonstrated that the professional activities in the endemic area were an indicator of the nature and intensity of contact with infested water [59].This fact has been also reported in the two villages of Itapinassu and São Joaquin in the county of Tracunhaém (state of Pernambuco) in Brazil [60].None other demographic factors analyzed were associated with S. mansoni compared to other studies which showed a significant association between intestinal schistosomiasis and age [12] or level of education [61].
Regarding diagnostical and clinical parameters, women who were not declared previous praziquantel treatment in the last six months were less infected with schistosomiasis than those reporting a history of schistosomiasis treatment.We assume that the first cases of women come from no endemic area such as the capital Dakar or Saint-Louis city or other cities of the central regions and recently arrived in the endemic area of Richard Toll.As the mass drug administration of Praziquantel targeted only school children, they may have never been treated since their first infection after they arrive in the study area.In the second case, it could be assumed that these women spent more time in the area and are more likely to be in permanent contact with infested waters.Other factors such as, the difference in the transmission dynamic of the disease, the type of water access frequented [45] and the lack of access to safe water for domestic activities could explain this difference [62].These results contrast with the study conducted by Dawaki et al. [63] in North Central Nigeria in Kano State.In this study, women with infection and treatment history were more infected than those who had never reported a history of infection.The present study showed that proteinuria was a risk factor associated to S. haematobium and S. mansoni infection in pregnant women.In addition to hematuria, this parameter could be considered a symptom of female genital schistosomiasis [64].This parameter could be taken into account in addition to hematuria which is the most important symptom and risk factor of female genital schistosomiasis [64].This will allow improving the detection of urogenital schistosomiasis in pregnant women in endemic areas.Low birth weights, total hemoglobin (THB), and blood group are not associated with schistosomiasis in this study.However, previous studies have demonstrated that pregnant women with urogenital schistosomiasis have an increased risk of low birth weight delivery [20] and increased risk of anemia was associated with a high level of S. mansoni infection [13].Other studies showed a close relationship between schistosomiasis and anemia caused by a fall in hemoglobin level [65].The availability of data on all the parameters studied in all participants would allow us to have a greater statistical strength and to get other parameters associated with schistosomiasis.

Conclusion
The presented study has revealed a high prevalence of urogenital schistosomiasis in pregnant women at Richard Toll in Senegal.Pregnant women who attended the public health facility of EPS were more infected than those attending the private health facility of the Senegalese Sugar Company.Molecular diagnostics by qPCR were more sensitive than the urine filtration and Kato-Katz techniques.More studies are needed to assess the real burden of schistosomiasis in pregnant women and the outcome of pregnancy.Moreover, implementing schistosomiasis surveillance even on the basis of haematuria and or proteinuria during antenatal care consultations to treat women to prevent pregnancy-related complications.
= 0.015) leukocyte detected by reagent trips in pregnant women urine were more likely associated with increased S. haematobium infection.The presence of nitrites and glucose on strips is not associated with S. haematobium infection.

Table 1
Descriptive analysis of all parameters collected among pregnant women in Richard Toll

Table 2
Prevalence of Schistosoma species according to microscopic and qPCR technique

Table 3
Sensitivity and specificity of quantitative real-time PCR (qPCR) compared to microscopy methods for the diagnostic of schistosomiasis

Table 4
Logistic regression bivariate analysis exploring factors associated with schistosomiasis cases among pregnant women (n = 298) in Richard Toll (Northern Senegal)

Table 5
Logistic regression multivariate analysis exploring factors associated with schistosomiasis cases among pregnant women (n = 298) in the health district of Richard Toll, in northern Senegal * Statistically significant